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Migration and distribution of two populations of hippocampal granule cell precursors during the perinatal and postnatal periods
Abstract
Methacrylate‐embedded sections and short‐survival thymidine radiograms of the hippocampal dentate gyrus were examined in perinatal and postnatal rats in order to trace the site of origin and migration of the precursors of granule cells and study the morphogenesis of the granular layer. The densely packed, spindle‐shaped cells of the secondary dentate matrix (a derivative of the primary dentate neuroepithelium) stream in a subpial position towards the granular layer of the internal dentate limb during the perinatal and early postnatal periods. By an accretionary process, the crest of the granular layer forms on day E21 and on the subsequent days the granular layer of the internal dentate limb expands progressively in a lateral direction. Granule cells differentiation, as judged by the transformation of polymorph, darkly staining small cells into rounder, lightly staining larger granule cells, follows the same gradient from the external dentate limb to the internal dentate limb. The secondary dentate matrix is in a process of dissolution by day P5. This matrix is the source of what will later become the outer shell of the granular layer composed of early generated granule cells. The thicker inner shell of the granular layer, formed during the infantile and juvenile periods, derives from an intrinsic, tertiary germinal matrix. On day E22, the dentate migration of the secondary dentate matrix becomes partitioned into two components: (a) the subpial component of extradentate origin, referred to in this context as the first dentate migration, and (b) the second dentate migration. The latter is distributed in the basal polymorph layer throughout the entire dentate gyrus and is henceforth recognized as the tertiary dentate matrix. The tertiary dentate matrix is prominent between days P3 and P10. It is postulated that the great increase in granule cell population during the infantile period is principally due to cells derived from this intrinsic matrix of the dentate gyrus. Between days P20 and P30 the tertiary dentate matrix disappears in the basal polymorph layer and henceforth proliferative cells become largely confined to the subgranular zone at the base of the granular layer. The subgranular zone is the source of granule cells produced during the juvenile and adult periods.
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“reduction in PTB triggered radial glial-like cells to convert into new granular neurons through what appears to be the typical developmental process by which new hippocampal neurons mature during development39 and in young adult animals40.”
From Therapeutically viable generation of neurons with antisense oligonucleotide suppression of PTB (2021) · cites this paper as [39]
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Cites
Autoradiographic and histological evidence of postnatal hippocampal neurogenesis in rats
Altman, J., & Das, G. D. (1965) · Journal of Comparative Neurology · doi:10.1002/cne.901240303 · Cited by 3,592
Self-citationBayer, S. A. (1980) · The Journal of Comparative Neurology · doi:10.1002/cne.901900107 · Cited by 913
Self-citationAutoradiographic investigation of cell proliferation in the brains of rats and cats
Altman, J. (1963) · The Anatomical Record · doi:10.1002/ar.1091450409 · Cited by 623
Self-citationTime of neuron origin in the hippocampal region. An autoradiographic study in the mouse.
Angevine, J. B. (1965) · PubMed · Cited by 476
Evidence that granule cells generated in the dentate gyrus of adult rats extend axonal projections
Stanfield, B. B., & Trice, J. (1988) · Experimental Brain Research · doi:10.1007/bf00250261 · Cited by 431
Altman, J., & Bayer, S. A. (1990) · The Journal of Comparative Neurology · doi:10.1002/cne.903010302 · Cited by 401
Self-citationBayer, S. A. (1982) · Experimental Brain Research · doi:10.1007/bf00238626 · Cited by 285
Self-citationEckenhoff, M. F., & RAKIC, P. T. (1984) · The Journal of Comparative Neurology · doi:10.1002/cne.902230102 · Cited by 239
Altman, J., & Bayer, S. A. (1990) · The Journal of Comparative Neurology · doi:10.1002/cne.903010303 · Cited by 198
Self-citationOn the number of neurons in the dentate gyrus of the rat
Boss, B. D., Peterson, G. M., & Cowan, W. M. (1985) · Brain Research · doi:10.1016/0006-8993(85)90257-4 · Cited by 178
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Kilpatrick, T. J., Cheema, S. S., Koblar, S. A., Tan, S. S., & Bartlett, P. F. (1994) · Neuroscience Letters · doi:10.1016/0304-3940(94)90576-2 · Cited by 13
Kadam, S. D., Mulholland, J. D., McDonald, J. W., & Comi, A. M. (2009) · Journal of Neuroscience Research · doi:10.1002/jnr.22109 · Cited by 12
Zetter, M. A., Roque, A., Hernández, V. S., Hernández‐Pérez, O. R., Gómora, M. J., Ruiz‐Velasco, S., Eiden, L. E., & Zhang, L. (2021) · Journal of Neuroendocrinology · doi:10.1111/jne.12969 · Cited by 13
Insights into isoform-specific mineralocorticoid receptor action in the hippocampus
Gaudenzi, C., Mifsud, K. R., & Reul, J. M. H. M. (2023) · Journal of Endocrinology · doi:10.1530/joe-22-0293 · Cited by 11
Eskandari, F., Salimi, M., Hedayati, M., & Zardooz, H. (2022) · Behavioural Brain Research · doi:10.1016/j.bbr.2022.113810 · Cited by 11
Effects of early environment on field CA2 pyramidal neurons in the guinea-pig
Bartesaghi, R., & Severi, S. (2003) · Neuroscience · doi:10.1016/j.neuroscience.2003.10.018 · Cited by 11
Gil, L., Chi-Ahumada, É., Niño, S. A., Capdeville, G., Méndez-Torres, A. M., Guerrero, C., Poves, A. B. R., Olazabal, I. M., & Jiménez-Capdeville, M. E. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms232112873 · Cited by 10
Radic, T., Al-Qaisi, O., Jungenitz, T., Beining, M., & Schwarzacher, S. W. (2015) · PLoS ONE · doi:10.1371/journal.pone.0135493 · Cited by 11
Jaskoll, T. F., & Melnick, M. (1999) · The Anatomical Record · doi:10.1002/(sici)1097-0185(19991101)256:3 · Cited by 153
Nandi, S., Alviña, K., Lituma, P. J., Castillo, P. E., & Hébert, J. M. (2017) · Neuroscience · doi:10.1016/j.neuroscience.2017.11.017 · Cited by 10
Xiao, X., Wu, J., Zhang, H., Wang, Y., Zhang, J., Liu, L., Yuchen, Minli, Yang, P., Wu, X., et al. (2020) · Brain and Behavior · doi:10.1002/brb3.1949 · Cited by 10
Li, Q., Cheng, D., Chen, R., Cai, Q., Jia, N., Su, Q., Zhang, H., Zhu, Z., Zeng, J., & Li, H. (2014) · Brain Research · doi:10.1016/j.brainres.2014.05.002 · Cited by 10
Li, M., Li, X., Zhang, X., Ren, J., Jiang, H., Wang, Y., Ma, Y., & Cheng, W. (2014) · International Journal of Developmental Neuroscience · doi:10.1016/j.ijdevneu.2014.02.004 · Cited by 10
Cardoso, A., Castro, J. P., Pereira, P. A., & Andrade, J. P. (2013) · Brain Research · doi:10.1016/j.brainres.2013.05.034 · Cited by 10
Trimpe, D. M., & Byrd-Jacobs, C. A. (2016) · Neuroscience · doi:10.1016/j.neuroscience.2016.06.026 · Cited by 10
Wasinski, F., Estrela, G. R., Arakaki, A. M., Bäder, M., Alenina, N. V., Klempin, F., & Araújo, R. C. (2016) · Frontiers in Neuroscience · doi:10.3389/fnins.2016.00402 · Cited by 10
Singular Adult Neural Stem Cells Do Not Exist
Petřík, D., Jörgensen, S. K. M., Eftychidis, V., & Siebzehnrübl, F. A. (2022) · Cells · doi:10.3390/cells11040722 · Cited by 13
Janeczko, K. J., Setkowicz, Z., Frączek, M., & Kochowska, J. (1999) · Brain Research · doi:10.1016/s0006-8993(98)01247-5 · Cited by 10
Fournier, N. M., Mach, Q. H., Whissell, P. D., & Persinger, M. A. (2012) · International Journal of Developmental Neuroscience · doi:10.1016/j.ijdevneu.2012.07.005 · Cited by 10
Petitto, J. M., Huang, Z. L., Meola, D., Ha, G. K., & Dauer, D. J. (2011) · Methods in molecular biology · doi:10.1007/978-1-61779-458-2_27 · Cited by 10
Counsell, J. R., Karda, R., Diaz, J. F. A., Carey, L., Wiktorowicz, T., Buckley, S. M. K., Ameri, S., Ng, J., Baruteau, J., Almeida, F., et al. (2018) · Molecular Therapy — Nucleic Acids · doi:10.1016/j.omtn.2018.07.006 · Cited by 10
Postnatal development of rat dentate gyrus: effects of methylazoxymethanol administration
Ciaroni, S., Cecchini, T., Ferri, P., Ambrogini, P., Cuppini, R., Lombardelli, G., Peruzzi, G., & Grande, P. D. (2002) · Mechanisms of Ageing and Development · doi:10.1016/s0047-6374(01)00359-1 · Cited by 10
Effects of early isolation on layer ii neurons in the entorhinal cortex of the guinea pig
Bartesaghi, R., Raffi, M., & Severi, S. (2003) · Neuroscience · doi:10.1016/s0306-4522(03)00354-3 · Cited by 10
Fonseca, M., Woodhams, P. L., Webb, M., Field, P. M., & Raisman, G. (1992) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.1992.tb00895.x · Cited by 10
Crofton, K. M., Gilbert, M. E., Friedman, K. P., DEMENEIX, B. A., Marty, M. S., & Zoeller, R. T. (2019) · OECD series on adverse outcome pathways · doi:10.1787/ea5aa069-en · Cited by 11
Human pluripotent stem cell-derived models of the hippocampus
Nishimura, H., & Li, Y. (2024) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/j.biocel.2024.106695 · Cited by 9
How Postnatal Insults May Program Development: Studies in Animal Models
Dalmaz, C., Noschang, C. G., Krolow, R., Raineki, C., & Lucion, A. B. (2014) · Advances in neurobiology · doi:10.1007/978-1-4939-1372-5_7 · Cited by 9
Gas1 is present in germinal niches of developing dentate gyrus and cortex
Estudillo, E., Zavala, P., Pérez‐Sánchez, G., Ayala‐Sarmiento, A. E., & Segovia, J. (2015) · Cell and Tissue Research · doi:10.1007/s00441-015-2338-x · Cited by 9
Exploration of the Brn4‐regulated genes enhancing adult hippocampal neurogenesis by RNA sequencing
Guo, J., Cheng, X., Zhang, L., Wang, L., Mao, Y., Tian, G., Xu, W., Wu, Y., Ma, Z., Qin, J., et al. (2017) · Journal of Neuroscience Research · doi:10.1002/jnr.24043 · Cited by 9
Briones, B. A., & Gould, E. (2019) · Elsevier eBooks · doi:10.1016/b978-0-12-813146-6.00007-2 · Cited by 9
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Pléau, C., Peret, A., Pearlstein, É., Scalfati, T., Vigier, A., Marti, G., Michel, F. J., Marissal, T., & Crépel, V. (2021) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2020.609123 · Cited by 9
Choices in surgical treatment of diverticulitis.
Lorenzetti, R., Cardin, F., Piatto, G., Mazzalai, F., Terranova, C., & Militello, C. (2012) · PubMed · doi:10.3275/8178 · Cited by 9
Bunk, E. C., König, H., Prehn, J. H. M., & Kirby, B. P. (2014) · Journal of Neuroscience Research · doi:10.1002/jnr.23347 · Cited by 9
Zheng, C., & Feng, L. (2006) · Journal of Cellular Physiology · doi:10.1002/jcp.20591 · Cited by 9
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Bayer, S. A. (2016) · The Journal of Comparative Neurology · doi:10.1002/cne.24058 · Cited by 9
Self-citationHarman, A. M. (1997) · Developmental Brain Research · doi:10.1016/s0165-3806(97)00134-x · Cited by 9
Kin Pong, U., Gao, L., Zhang, H., Ji, Z., Lin, J., Peng, S., Zhang, X., Xue, S., Qin, W., Tsang, L. L., et al. (2025) · Cell Death and Differentiation · doi:10.1038/s41418-025-01470-2 · Cited by 8
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Gate, D., Danielpour, M., Levy, R., Breunig, J. J., & Town, T. (2012) · Molecular Neurobiology · doi:10.1007/s12035-012-8276-7 · Cited by 8
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Nakafuku, M., & Grande, A. W. (2013) · Elsevier eBooks · doi:10.1016/b978-0-12-397265-1.00074-5 · Cited by 8
Miyata, M., Maruo, T., Kaito, A., Wang, S., Yamamoto, H., Fujiwara, T., Mizoguchi, A., Mandai, K., & Takai, Y. (2016) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2016.12.007 · Cited by 9
Gustus, K., Lozano, E., Newville, J., Li, L., Valenzuela, C. F., & Cunningham, L. A. (2019) · Alcoholism Clinical and Experimental Research · doi:10.1111/acer.14207 · Cited by 8
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Kong, X., Shu, X., Wang, J., Liu, D., Ni, Y., Zhao, W., Wang, L., Gao, Z., Chen, J., Yang, B., et al. (2022) · Development · doi:10.1242/dev.201286 · Cited by 8
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Seki, T. (2011) · Springer eBooks · doi:10.1007/978-4-431-53933-9_7 · Cited by 9
Matsufuji, M., Utsunomiya, H., Inoue, T., Yasumoto, S., Takashima, S., & Mitsudome, A. (2011) · Pediatrics International · doi:10.1111/j.1442-200x.2011.03444.x · Cited by 8
Synchronized spike waves in immature dentate gyrus networks
Seki, M., Kobayashi, C., Takahashi, N., Matsuki, N., & Ikegaya, Y. (2012) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2012.07995.x · Cited by 8
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Sancho-Bielsa, F. J., Navarro‐López, J. D., Alonso‐Llosà, G., Molowny, A., Ponsoda, X., Yajeya, J., & López‐García, C. (2012) · PLoS ONE · doi:10.1371/journal.pone.0048470 · Cited by 8
Imura, T., Kobayashi, Y., Suzutani, K., Ichikawa‐Tomikawa, N., & Chiba, H. (2018) · Hippocampus · doi:10.1002/hipo.23045 · Cited by 9
Laminar organization of the mouse dentate gyrus: Insights from BETA2/Neuro D mutant mice
Turco, D. D., Gebhardt, C., Burbach, G. J., Pleasure, S. J., Lowenstein, D. H., & Deller, T. (2004) · The Journal of Comparative Neurology · doi:10.1002/cne.20239 · Cited by 8
Environmental Control of the Survival and Differentiation of Dentate Granule Neurons
Kim, J. (2004) · Cerebral Cortex · doi:10.1093/cercor/bhh096 · Cited by 8
Emili, M., Stagni, F., Russo, C. A., Angelozzi, L., Guidi, S., & Bartesaghi, R. (2024) · Neuropharmacology · doi:10.1016/j.neuropharm.2024.110170 · Cited by 7
Namba, T., Shinohara, H. M., & Seki, T. (2019) · Brain Structure and Function · doi:10.1007/s00429-019-01971-0 · Cited by 6
Rostami, F., Javan, M., Moghimi, A., Haddad‐Mashadrizeh, A., & Fereidoni, M. (2019) · Life Sciences · doi:10.1016/j.lfs.2019.117154 · Cited by 7
Machaalani, R., Vivekanandarajah, A., Despotovski, V., Rodriguez, M. L., & Waters, K. A. (2021) · Journal of Neuropathology & Experimental Neurology · doi:10.1093/jnen/nlab119 · Cited by 7
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Sourial-Bassillious, N., Eklöf, A., Scott, L., Aperia, A. C., & Zelenin, S. M. (2006) · Pediatric Research · doi:10.1203/01.pdr.0000238246.74817.a0 · Cited by 7
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Vogler, S., Prokoph, S., Freudenberg, U., Binner, M., Tsurkan, M. V., Werner, C., & Kempermann, G. (2018) · Scientific Reports · doi:10.1038/s41598-018-26417-1 · Cited by 7
Giralt, A., Brito, V., Pardo, M., Rubio, S. E., Marion‐Poll, L., Martín‐Ibáñez, R., Zamora‐Moratalla, A., Bosch, C., Ballesteros, J. J., Blasco, E., et al. (2019) · Experimental Neurology · doi:10.1016/j.expneurol.2019.113095 · Cited by 7
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Blume, M., Inoguchi, F., Sugiyama, T., Owada, Y., Osumi, N., Aimi, Y., Taki, K., & Katsuyama, Y. (2017) · Development Growth & Differentiation · doi:10.1111/dgd.12393 · Cited by 7
Arafat, E. A.-G., & Shabaan, D. A. (2019) · Biotechnic & Histochemistry · doi:10.1080/10520295.2019.1637021 · Cited by 7
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Setkowicz, Z., Pawliński, R., Ziaja, M., & Janeczko, K. J. (1999) · International Journal of Developmental Neuroscience · doi:10.1016/s0736-5748(99)00014-3 · Cited by 7
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Blackstad, J. S., Osen, K. K., & Leergaard, T. B. (2022) · Hippocampus · doi:10.1002/hipo.23457 · Cited by 5
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Quadros, A. R. A. D. A., Arazola, R. D., Álvarez, A. R., Pires, J., Meredith, R. M., Saarloos, I., Verhage, M., & Toonen, R. F. G. (2022) · iScience · doi:10.1016/j.isci.2022.104069 · Cited by 6
Schaeffer, E. L. (2010) · Archives of Clinical Psychiatry (São Paulo) · doi:10.1590/s0101-60832010000200008 · Cited by 7
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Porter, N. M., Herman, J. P., & Landfield, P. W. (2001) · Comprehensive physiology · doi:10.1002/cphy.cp070414 · Cited by 6
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Parichha, A., Datta, D., Suresh, V., Chatterjee, M., Holtzman, M. J., & Tole, S. (2022) · Development · doi:10.1242/dev.200953 · Cited by 5
Pastor-Alonso, O., Zahra, A. S., Kaske, B., García‐Moreno, F., Tetzlaff, F., Bockelmann, E., Grunwald, V., Martín‐Suárez, S., Riecken, K., Witte, O. W., et al. (2023) · The EMBO Journal · doi:10.1038/s44318-023-00011-2 · Cited by 9
Bouargane, Z., Moubarrad, F. L., Anouar, Y., Boukhzar, L., Bennis, M., & Ba-M’hamed, S. (2025) · Hippocampus · doi:10.1002/hipo.70024 · Cited by 5
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Durens, M., Soliman, M., Millonig, J. H., & DiCicco-Bloom, E. M. (2021) · Developmental Neurobiology · doi:10.1002/dneu.22824 · Cited by 5
Bashford, A. L., & Subramanian, V. (2022) · Human Molecular Genetics · doi:10.1093/hmg/ddac095 · Cited by 5
Hernandez-Lopez, J. M., Hernandez-Medina, C., Medina-Corvalan, C., Rodenas, M., Almagro‐García, F., Pérez-García, C., Echevarría, D., Martínez-Carratalá, F. A., Geijo‐Barrientos, E., & Martínez, S. (2023) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-023-04787-8 · Cited by 7
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Hernandez, M., Ghislin, S., Lalonde, R., & Strazielle, C. (2023) · Neurochemistry International · doi:10.1016/j.neuint.2023.105611 · Cited by 5
Cifre, M., Palou, A., & Oliver, P. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms25010228 · Cited by 5
Kirschen, G. W., Antonio, A. D., & Ge, S. (2016) · Elsevier eBooks · doi:10.1016/b978-0-12-801977-1.00002-7 · Cited by 5
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Neurogenesis in the adult rat hippocampus: lesion stimulated phenomenon?
Skup, M., Herrera, D. G., Ribeiro‐da‐Silva, A., & Cuello, A. C. (1993) · Elsevier eBooks · doi:10.1016/b978-0-444-81470-8.50026-0 · Cited by 5
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Saitô, H., Kato, R., Hashimoto, T., Uchida, Y., Hase, T., Tsuruga, K., Takita, K., & Morimoto, Y. (2018) · Biomedical Research · doi:10.2220/biomedres.39.39 · Cited by 5
Xia, Y., Zhang, Y., Xu, M., Zou, X., Gao, J., Ji, M., & Chen, G. (2022) · Development · doi:10.1242/dev.200272 · Cited by 4
Machaalani, R., Rodriguez, M. L., & Vivekanandarajah, A. (2024) · Journal of Neuropathology & Experimental Neurology · doi:10.1093/jnen/nlae109 · Cited by 4
Schaeffer, E. L., Cerulli, F. G., de Souza, H. O. X., Catanozi, S., & Gattaz, W. F. (2014) · Journal of Neural Transmission · doi:10.1007/s00702-014-1175-5 · Cited by 4
Abbasi, Z., Rassouli, F. B., Seno, M. M. G., & Fereidoni, M. (2017) · Neuroscience Research · doi:10.1016/j.neures.2017.10.003 · Cited by 4
Pimentel, H. D. C., Macêdo-Lima, M., Viola, G. G., Melleu, F. F., dos Santos, T. S., Franco, H. S., da Silva, R. D. S., de Oliveira, C. L., Marino–Neto, J., dos Santos, J. R., et al. (2020) · Journal of Chemical Neuroanatomy · doi:10.1016/j.jchemneu.2020.101901 · Cited by 4
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Uchida, Y., HASHIMOTO, T., Saitô, H., Takita, K., & Morimoto, Y. (2022) · Biomedical Research · doi:10.2220/biomedres.43.1 · Cited by 4
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Rahim, R. S., John, J. A. S., Crane, D. I., & Meedeniya, A. C. B. (2017) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2017.11.015 · Cited by 5
Wei, K., Chen, P., Shen, F.-Y., Zhang, Y., Liu, Y., Wang, Z.-R., Loepke, A. W., Wang, Y., & Deng, M. (2019) · Neuroscience · doi:10.1016/j.neuroscience.2019.07.009 · Cited by 4
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Zhao, Z., Li, B., Wu, Y., Chen, X., Guo, Y., Shen, Y., & Huang, H. (2019) · BMC Neuroscience · doi:10.1186/s12868-019-0542-4 · Cited by 4
Guzman, R. M. D., Medina, J., Saulsbery, A. I., & Workman, J. L. (2020) · Physiology & Behavior · doi:10.1016/j.physbeh.2020.113106 · Cited by 4
Orr, A. G., Sharma, A. K., Binder, N. B., Miller, A. H., & Pearce, B. D. (2009) · Journal of Molecular Neuroscience · doi:10.1007/s12031-009-9293-5 · Cited by 4
Kawakita, A., Yamashita, T., Taniguchi, M., Koyama, Y., Kubo, T., Tsuji, L., & Tohyama, M. (2003) · Developmental Brain Research · doi:10.1016/s0165-3806(03)00169-x · Cited by 4
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Metadata
- Authors
- Altman, J., & Bayer, S. A.
- Affiliations
- Purdue University West Lafayette (US)
- Indiana University – Purdue University Indianapolis (US)
- Venue
- Journal of Comparative Neurology
- Publisher
- Wiley
- Published
- 1990-11-15
- Volume
- 301
- Issue
- 3
- Pages
- 365-381
- ISSN
- 0021-9967 (ISSN-L)
- 1096-9861
- OpenAlex
- W2006624547
- Cited by
- 819
- References
- 12
- Citations by year
- 2026: 8 · 2025: 11 · 2024: 9 · 2023: 9 · 2022: 18 · 2021: 17 · 2020: 24 · 2019: 29 · 2018: 28 · 2017: 37 · 2016: 33 · 2015: 35 · 2014: 31 · 2013: 35 · 2012: 39
- FWCI
- 3.40
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- The Journal of Comparative Neurology (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Developmental Biology and Gene Regulation
- Keywords
- hippocampal granule cells, granule cell precursors, dentate gyrus, subgranular zone, perinatal development, postnatal development, cell migration, granule cell differentiation
- MeSH terms
- Aging, Animals, Autoradiography, Cell Differentiation, Cell Division, Cell Movement, Gestational Age, Hippocampus, Morphogenesis, Rats, Inbred Strains, Thymidine, Tritium, Rats
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